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NCT ID: NCT00476814 Not yet recruiting - Clinical trials for Primary Sclerosing Cholangitis

NPD Measurements in PSC Patients

Start date: n/a
Phase: N/A
Study type: Observational

Primary Sclerosing Cholangitis (PSC) is a chronic disorder of the liver causing jaundice and liver damage. When Cystic Fibrosis affects the liver, the damaged liver looks like the liver in PSC. This study is designed to answer the question whether isolated PSC may be a form of CF only in the liver

NCT ID: NCT00478998 Not yet recruiting - Clinical trials for Upper Tract Ureterolithiasis

Comparing Patients After ESWL Treated With Ureteral Stents Versus Expulsion Therapy With Tamsulosin

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see whether patients undergoing ESWL, for upper tract urinary stones between 1.5-2.0cm, may be treated by expulsion therapy(Tamsulosin) instead of inserting ureteral stents .

NCT ID: NCT00484224 Not yet recruiting - Hearing Loss Clinical Trials

Audiological Disturbances in Vitiligo

Start date: n/a
Phase: N/A
Study type: Observational

The purpose of this study is to determine wether vitiligo patients have more audiological abmnormalities, than the healthy population.

NCT ID: NCT00491413 Not yet recruiting - Asphyxia Clinical Trials

Erythropoietin for Infants With Brain Injuries Due to Oxygen Deprivation at Birth

Start date: n/a
Phase: Phase 1
Study type: Interventional

Erythropoietin (Epo) is a hormone normally found in the body that may protect brain cells from damage due to lack of oxygen. This study will evaluate the safety of high-dose Epo in infants who did not get enough oxygen during birth.

NCT ID: NCT00492674 Not yet recruiting - Knee Osteoarthritis Clinical Trials

The Effect of Perioperative Neuromuscular Training on the Outcome of Total Knee Arthroplasty

Start date: n/a
Phase: N/A
Study type: Interventional

Introduction: Total knee arthroplasty (TKA) is a consensus treatment for end-stage knee osteoarthritis. The peri-operative rehabilitation is an important part of the outcome of such procedure. Previous studies have shown that there is correlation between both pre-operative functional status and the intensiveness of the post-operative rehabilitation to the post operative function of the patient. An important part of the peri-operative rehabilitation in TKA is the neuromuscular control re-education. A novel biomechanical device comprising of four individually calibrated elements attached onto foot-worn platforms was recently developed. This device is capable of bringing the patient to a functional bio-mechanical alignment during standing and walking, while simultaneously strengthening dynamic stabilizers and training neuromuscular control by means of controlled biomechanical perturbations. Objectives: The aim of this study is to evaluate the influence of pre and post operative training with the biomechanical device mentioned above on the functional outcome and quality of life of patients undergoing TKA. Design and Setting: Randomized, controlled and double blind prospective trial Patients: 120 patients who are candidates to TKA Interventions: Patients will randomly assigned into five groups (active, sham and control) and will followed for fourteen months (two moths pre-operative and twelve months post-operative). All groups will undergo post-operative physical therapy (PT) according to the standard guidelines. In addition, the active groups will be treated with the device and its four biomechanical elements that had been individually calibrated for each patient. The sham group will be treated with the same device; however, the biomechanical elements will have zero perturbation and will be positioned along the central longitudinal line of the shoe-platform. The control group will be treated only according to the standard post-operative protocol. The five groups: 1. Pre- operative BD training and post-operative PT and BD training 2. Pre- operative sham training and post-operative PT and BD training 3. Pre- operative sham training and post-operative PT and sham training 4. No pre-operative training (according to the guidelines in Israel) and post-operative PT and BD training. 5. No pre-operative training (according to the guidelines in Israel) and post-operative PT and sham training. Primary Outcome Measures: Spatio-temporal measures (recorded by Gait-Rite™) and the Aggregated Locomotor Function (ALF) assessment. Secondary Outcome Measures: Pain and function questionnaire measured by the Western Ontario and McMaster Osteoarthritis Index (WOMAC) and Quality of life will be evaluated by the SF-36 quality of life questionnaire. Measurements will be taken at day-1 (two months before the TKA) and at four more stations: 1 Week prior to the TKA, Three months post the TKA, six months post the TKA and twelve months post the TKA

NCT ID: NCT00497042 Not yet recruiting - Clinical trials for Teeth, Endodontically-Treated

Safety and Efficacy of Using the Endodontic Self Adjusting File - SAF for Root Canal Treatment

Start date: n/a
Phase: N/A
Study type: Interventional

The study’s primary goal is to assess the safety of the SAF (Self Adjusting File) device for root canal treatments. The study’s secondary goal is to evaluate the effectiveness of the SAF device for root canal treatments

NCT ID: NCT00502437 Not yet recruiting - Antiemetic Clinical Trials

The Antigagging Effect of Granisetron (Kytril), an Antiemetic Drug, in Dental Situations

Start date: n/a
Phase: N/A
Study type: Interventional

Antigagging effect of kytril (granisetron) an antiemetic drug in dental situations Gagging in dental situations can be a problem to the patient and the operating dentist. There are not proven methods of eliminating this reflex which sometimes will not allow routine quality dental care. Pharmacological and behavioral approaches to eliminate this reflex have been tried with limited success. This suggested study will test a potent antiemetic drug used in other clinical situations such as antineoplastic treatment. Granisetron is a potential antagonist for the 5-hydroxytryptamine3-receptor - 5HT(3), The drug binds to the receptor and blocks the effect of nausea and vomiting. Kytril mechanism of action was successfully proven for various medical situations as a potential antiemetic agent. Our Center for dental sedation and anesthesia in the oral medicine department have received approval to use Granisetron as an antigagging drug in dental situations based on several pilot studies conducted in other medical centers in different clinical situations such as strabismus corrections, post hysterectomy and others. Our preliminary clinical impression is that pre-emptive IV administration of this drug to patients with increased gag reflex is beneficial. In our research we try to investigate the possibility of using kytril in dental situations. In the first stage of this research we will study the INTRAVENOUS use of this drug and its effects On normal subjects compare them to themselves with placebo. According to the results of this study we will go on to the second stage of the research and try the same drug under oral administration. The purpose of this study is to test the antigagging effect of this drug in a controlled manner in dental situations. Our working hypothesis is that administration of this drug in dental situations with success, will allow many patients to receive good dental care

NCT ID: NCT00507052 Not yet recruiting - Hemodialysis Clinical Trials

Effect of N-Acetylcysteine on Residual Renal Function in Chronic Hemodialysis Patients

Start date: n/a
Phase: N/A
Study type: Interventional

In our opinion, it is worth to check an ability of antioxidant therapy to produce a favorable effect on Residual Renal Function. The aim of our study is to investigate the effect of N-acetylsysteine on RRF in prevalent HD patients.

NCT ID: NCT00507364 Not yet recruiting - Clinical trials for Interventional Study

Treatment of Anal Fissure by Activated Human Macrophages

Start date: n/a
Phase: Phase 3
Study type: Interventional

Chronic anal fissure is a linear tear in the distal anal canal. Most chronic fissures require intervention to heal. Surgical sphincterotomy is currently performed. However, the procedure permanently weakens the internal sphincter and may be associated with permanent complications such as incontinence. Current topical treatment or " chemical sphincterotomy" is effective in the short term for about 70% of the patient more than 50% of them will suffer from recurrence. Number of studies support the hypothesis that local ischemia is the reason for failure to heal in anal fissure. Treatment of refractory wounds by macrophage suspension is an innovative method since 1995, macrophage suspensions have been used successfully in more than 1400 patients in several hospitals in Israel without any side effect.Macrophages have key function in almost every stage of wound healing. They help in the digestion of bacteria, in a later stage, they secret IL-6, which influences endothelial cell proliferation and the initiation of angiogenesis. The study hypothesis is that local injection of activated human macrophages into chronic anal fissure may induce fissure healing.

NCT ID: NCT00531154 Not yet recruiting - Obesity Clinical Trials

Evaluation of the Dental Health Condition in Obesity Patients Before and After Bariatric Surgery

Start date: n/a
Phase: N/A
Study type: Observational

The aim of this study is to investigate whether there was an association between obesity and periodontitis, tendency to caries and periapical lesions. People who have a higher body mass index produce cytokines (hormone-like proteins), that lead to systemic/chronic inflammation (like periodontitis and periapical lesions), and obesity related dietary habits could result in an increment of dental caries because both the amount and the frequency of sucrose ingestion are important factors associated with the aetiology of the oral disease.